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Author Details

Frank Dudbridge
2000
191
59
PMIDPaper TitleJournal TitlePublished Year
37537942Reassessing the association of MUC5B with survival in idiopathic pulmonary fibrosis.2023
35537820Mendelian randomisation of eosinophils and other cell types in relation to lung function and disease.Thorax2023
37749248Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.Nat Genet2023
37579195Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.Genetics2023
37962983Epigenome-wide association study shows differential DNA methylation of MDC1, KLF9 and CUTA in autoimmune thyroid disease.2023
37872160Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease.2023
37093672Causal inference methods for intergenerational research using observational data.2023
36744935DeepPheWAS: an R package for phenotype generation and association analysis for phenome-wide association studies.2023
37167572Family Matters: Germline Testing in Thoracic Cancers.Am Soc Clin Oncol Educ Book2023
35347715Research Review: How to interpret associations between polygenic scores, environmental risks, and phenotypes.Journal of Child Psychology and Psychiatry and Allied Disciplines2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35583096Adjusting for collider bias in genetic association studies using instrumental variable methods.Genet Epidemiol2022
36163213Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank.Nutrition, Metabolism and Cardiovascular Diseases2022
35274198Applying Mendelian randomization to appraise causality in relationships between nutrition and cancer.Cancer Causes Control2022
35110547A robust method for collider bias correction in conditional genome-wide association studies.Nat Commun2022
35105882The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples.Nat Commun2022
34524976Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3.European Journal of Endocrinology2021
32229610Polygenic Mendelian Randomization.Cold Spring Harbor Perspectives in Medicine2021
33484127Epigenome-Wide Association Study of Thyroid Function Traits Identifies Novel Associations of fT3 With KLF9 and DOT1L.J Clin Endocrinol Metab2021
34290290Genetic overlap and causal associations between smoking behaviours and mental health.Scientific Reports2021
33741915Clonal architecture in mesothelioma is prognostic and shapes the tumour microenvironment.Nat Commun2021
34115765Genetic sensitivity analysis: Adjusting for genetic confounding in epidemiological associations.PLoS Genet2021
33837305Identifying high-confidence capture Hi-C interactions using CHiCANE.Nat Protoc2021
34099722Author Correction: Clonal architecture in mesothelioma is prognostic and shapes the tumour microenvironment.Nat Commun2021
33444330Polygenic risk scores in cardiovascular risk prediction: A cohort study and modelling analyses.PLoS Med2021
34247229Mortality risk comparing walking pace to handgrip strength and a healthy lifestyle: A UK Biobank study.European Journal of Preventive Cardiology2021
33226834Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations.American Journal of Respiratory and Critical Care Medicine2021
33221865Are there causal relationships between attention-deficit/hyperactivity disorder and body mass index? Evidence from multiple genetically informed designs.International Journal of Epidemiology2021
34913977Interaction of Cigarette Smoking and Polygenic Risk Score on Reduced Lung Function.JAMA Netw Open2021
34370750Exploiting collider bias to apply two-sample summary data Mendelian randomization methods to one-sample individual level data.PLoS Genet2021
34698370Impact of past obstetric history and cervical excision on preterm birth rate.Acta Obstetricia et Gynecologica Scandinavica2021
34416156Robust genetic nurture effects on education: A systematic review and meta-analysis based on 38,654 families across 8 cohorts.American Journal of Human Genetics2021
33173067Author Correction: Genome-wide association study of self-reported walking pace suggests beneficial effects of brisk walking on health and survival.Communications Biology2020
31910697Family history of pre-eclampsia and cardiovascular disease as risk factors for pre-eclampsia: the GenPE case-control study.Hypertension in Pregnancy2020
31680049Replication of Newly Identified Genetic Associations Between Abdominal Aortic Aneurysm and SMYD2, LINC00540, PCIF1/MMP9/ZNF335, and ERG.Eur J Vasc Endovasc Surg2020
31995593Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach.PLoS One2020
32219344Polygenic risk scores for coronary artery disease and subsequent event risk amongst established cases.Hum Mol Genet2020
32216834Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts.2020
32152294Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders.Translational Psychiatry2020
32654539Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data.Circulation2020
32594841Criteria for evaluating risk prediction of multiple outcomes.Statistical Methods in Medical Research2020
33239407Relative contributions of family history and a polygenic risk score on COPD and related outcomes: COPDGene and ECLIPSE studies.BMJ Open Respir Res2020
33128006Genome-wide association study of self-reported walking pace suggests beneficial effects of brisk walking on health and survival.Communications Biology2020
31545794Robust methods in Mendelian randomization via penalization of heterogeneous causal estimates.PLoS One2019
31719968RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation.Mol Autism2019
30705363Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone.Scientific Reports2019
30804560New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.Nat Genet2019
30952951Adjustment for index event bias in genome-wide association studies of subsequent events.Nature Communications2019
30897348Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.Circ Genom Precis Med2019
30942833Multi-Polygenic Score Approach to Identifying Individual Vulnerabilities Associated With the Risk of Exposure to Bullying.JAMA Psychiatry2019
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